Canonical Allele Identifier: CA1752440889
Gene: NOS3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151011007G= , CM000669.2:g.151011007G= GRCh38
NC_000007.13:g.150708095G= , CM000669.1:g.150708095G= GRCh37
NC_000007.12:g.150339028G= NCBI36
NG_011992.1:g.24949G=
NG_030317.1:g.18493C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297494.8:c.2984+21G= MANE Select ENSP00000297494.3:n.2984+21G=
ENST00000297494.7:c.2984+21G= ENSP00000297494.3:n.2984+21G=
ENST00000461406.5:c.2366+21G= ENSP00000417143.1:n.2366+21G=
ENST00000468293.5:n.467+21G=
ENST00000475017.1:c.865+21G=
ENST00000477227.1:n.363+21G=
NM_000603.4:c.2984+21G= NP_000594.2:n.2984+21G=
NM_000603.5:c.2984+21G= MANE Select NP_000594.2:n.2984+21G=
Search 100 bp 5'
Search 100 bp 3'